Iron oxide nanoparticle core-shell magnetic microspheres: Applications toward targeted drug delivery

被引:35
作者
Ayyanaar, Srinivasan [1 ]
Kesavan, Mookkandi Palsamy [2 ]
Balachandran, Chandrasekar [3 ]
Rasala, Swetha [4 ]
Rameshkumar, Perumal [5 ]
Aoki, Shin [3 ,6 ]
Rajesh, Jegathalaprathaban [7 ]
Webster, Thomas J. [8 ]
Rajagopal, Gurusamy [1 ]
机构
[1] Chikkanna Govt Arts Coll, PG & Res Dept Chem, Tiruppur, Tamil Nadu, India
[2] Hajee Karutha Rowther Howdia Coll, Dept Chem, Uthamapalayam, Tamil Nadu, India
[3] Tokyo Univ Sci, Fac Pharmaceut Sci, Noda, Chiba, Japan
[4] Natl Univ Ireland Galway, Ctr Res Med Devices CURAM, Galway, Ireland
[5] Kalasalingam Acad Res & Educ, Dept Chem, Krishnankoil, Tamil Nadu, India
[6] Tokyo Univ Sci, Res Inst Sci & Technol, Noda, Chiba, Japan
[7] Mohamed Sathak Engn Coll, Chem Res Ctr, Kilakarai, Tamil Nadu, India
[8] Northeastern Univ, Dept Chem Engn, Boston, MA 02115 USA
关键词
Poly(D; L-lactide-co-glycolic acid); Lecithin; Magnetic core microsphere; Cytotoxicity; Targeted drug delivery; OXIDATIVE STRESS; CANCER-CELLS; ROS; MICROCAPSULES; ADSORPTION; EFFICIENCY; COMPLEXES; POLYMERS; REMOVAL; RELEASE;
D O I
10.1016/j.nano.2019.102134
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
This study describes a sensitive reactive oxygen species (ROS)-responsive lecithin (LEC) incorporated iron oxide nanoparticle (Fe3O4 NP) system with potent anti-inflammatory properties and even more so when the antioxidant drug curcumin (CUR) is encapsulated in the PLGA hybrid magnetic microsphere system (Fe3O4@LEC-CUR-PLGA-MMS). The delivery system is responsive to ROS including an H2O2 environment to release the payload (CUR) drug. Greater cytotoxicity properties were observed in the presence of Fe3O4@LEC-CUR-PLGA-MMS against A549 and HeLa S3 cells with IC50 values after 24 h of 10 and 12 mu g/mL and 10 and 20 mu g/mL, respectively. The present Fe3O4@LEC-CUR-PLGA-MMS system demonstrated much better in vitro cytotoxicity, cellular morphological changes and moreover an ability to limit colony formation for A549 and HeLa S3 cancer cell lines than non-cancerous cells, and thus, should be further studied for a wide range of medical applications. (C) 2019 Elsevier Inc. All rights reserved.
引用
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页数:11
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